Core principles

EmRQ Limited was set up in October 2024 by Emma Barringer, who observed consistent challenges and gaps having had a seasoned career across the IVD pathway with a focus on QARA and Clinical.

Now, through personal expertise and by collaborating with industry partners and other seasoned professionals, EmRQ Limited has identified service offerings to IVD manufacturers that will complete these challenges and close the gaps. 

We are passionate about supporting IVD professionals through their device journey. It’s those little things day to day - sometimes you don’t know what you don’t know. Luckily, we can help you! Whether it’s sharing our own personal expertise or through our very trusted partners, we can provide support cross-functionally, end-to-end to ensure your journey is a smooth one.

With previous experience in the public healthcare sector laboratories, we also understand the importance of getting awesome innovations out there to patients.

I’m Emma Barringer, an IVD Consultant with over 24 years of experience in Quality, Regulatory, and Clinical Affairs within the In-Vitro Diagnostic (IVD) and Medical Device industries. I have a deep understanding of the entire product pathway, from development and regulatory compliance to post-market surveillance.

Currently, I work as a Director and Consultant at EmRQ Limited, where I help guide IVD companies through the complexities of product planning, performance evaluations, and regulatory requirements. I’m passionate about driving continuous improvement and cultural change within organizations, and I believe strongly in the power of mentoring teams to help them reach their full potential and also the business potential.

Throughout my career, I’ve held senior leadership roles, including Head of QARA & Clinical Affairs at Novacyt Group, where I was responsible for regulatory and clinical activities across multiple sites. I’ve developed expertise in strategic regulatory planning, clinical study documentation, and ensuring compliance with industry regulations/standards like ISO and IVDR. I thrive on collaborating with multidisciplinary teams to deliver successful product outcomes.

I’m committed to providing expert guidance, unlocking the potential in people and organisations, and ensuring compliance success in everything I do